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Disease Ontology Browser
Joubert syndrome 21 (DOID:0110990)
Alliance: disease page
Synonyms: JBTS21
Alt IDs: OMIM:615636
Definition: A Joubert syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CSPP1 gene on chromosome 8q13.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.13
The Jackson Laboratory